[Biological treatment of multiple sclerosis]

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

[Biological treatment of multiple sclerosis]. / Sorensen, P.S.; Sellebjerg, F.

I: Ugeskrift for læger, Bind 170, Nr. 24, 2008, s. 2156-2159.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Sorensen, PS & Sellebjerg, F 2008, '[Biological treatment of multiple sclerosis]', Ugeskrift for læger, bind 170, nr. 24, s. 2156-2159.

APA

Sorensen, P. S., & Sellebjerg, F. (2008). [Biological treatment of multiple sclerosis]. Ugeskrift for læger, 170(24), 2156-2159.

Vancouver

Sorensen PS, Sellebjerg F. [Biological treatment of multiple sclerosis]. Ugeskrift for læger. 2008;170(24):2156-2159.

Author

Sorensen, P.S. ; Sellebjerg, F. / [Biological treatment of multiple sclerosis]. I: Ugeskrift for læger. 2008 ; Bind 170, Nr. 24. s. 2156-2159.

Bibtex

@article{6159f9509c6511debc73000ea68e967b,
title = "[Biological treatment of multiple sclerosis]",
abstract = "In 1996 interferon (IFN)beta was the first biopharmaceutical product to be approved for the treatment of relapsing-remitting multiple sclerosis (MS). In 2006 the more potent monoclonal antibody natalizumab was approved. Presently, a number of monoclonal antibodies are being studied, including alemtuzumab, daclizumab and rituximab, which have all shown promising results. However, the monoclonal antibodies generally have a less favourable safety profile and are more expensive than the currently used first-line therapies, IFNb and glatiramer acetate Udgivelsesdato: 2008/6/9",
author = "P.S. Sorensen and F. Sellebjerg",
year = "2008",
language = "Dansk",
volume = "170",
pages = "2156--2159",
journal = "Ugeskrift for Laeger",
issn = "0041-5782",
publisher = "Almindelige Danske Laegeforening",
number = "24",

}

RIS

TY - JOUR

T1 - [Biological treatment of multiple sclerosis]

AU - Sorensen, P.S.

AU - Sellebjerg, F.

PY - 2008

Y1 - 2008

N2 - In 1996 interferon (IFN)beta was the first biopharmaceutical product to be approved for the treatment of relapsing-remitting multiple sclerosis (MS). In 2006 the more potent monoclonal antibody natalizumab was approved. Presently, a number of monoclonal antibodies are being studied, including alemtuzumab, daclizumab and rituximab, which have all shown promising results. However, the monoclonal antibodies generally have a less favourable safety profile and are more expensive than the currently used first-line therapies, IFNb and glatiramer acetate Udgivelsesdato: 2008/6/9

AB - In 1996 interferon (IFN)beta was the first biopharmaceutical product to be approved for the treatment of relapsing-remitting multiple sclerosis (MS). In 2006 the more potent monoclonal antibody natalizumab was approved. Presently, a number of monoclonal antibodies are being studied, including alemtuzumab, daclizumab and rituximab, which have all shown promising results. However, the monoclonal antibodies generally have a less favourable safety profile and are more expensive than the currently used first-line therapies, IFNb and glatiramer acetate Udgivelsesdato: 2008/6/9

M3 - Tidsskriftartikel

VL - 170

SP - 2156

EP - 2159

JO - Ugeskrift for Laeger

JF - Ugeskrift for Laeger

SN - 0041-5782

IS - 24

ER -

ID: 14276965